Matches in Nanopublications for { ?s ?p "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.
- NP329447.RAhjxb4ID-cQU8QX3IUT05vN5vFAd_6YSwEv7EPV-ndCQ130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329447.RAhjxb4ID-cQU8QX3IUT05vN5vFAd_6YSwEv7EPV-ndCQ130_provenance.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.
- NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748697.RA4AfYc2GQpNnAr7DrmCBRmZE6W7vGBw127XuoHx-aw4A130_provenance.